Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Company hidden предлагает практический опыт работы с системами биопроизводства, наставничество и полезные межфункциональные проекты, но широкий диапазон оплаты и строгие требования к работе на месте и статусу U.S. person ограничивают определённость и доступность вакансии.
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Разброс оплатыОграничения по допускуАктуальные инструментыБиотехнологииПрактический опыт
Оценка от Hirify AI
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Co-Op, Automation, Digital Manufacturing & Controls (Biotech): Supporting digital, automation, controls, software, and data systems for regulated biopharmaceutical manufacturing with an accent on manufacturing data, system integrations, dashboards, and GMP computerized systems. Focus on developing and testing applications, APIs, integrations, and automation solutions, troubleshooting data flows, and validating systems in a site-based manufacturing environment.
Location: Norwood, Massachusetts, United States; 100% onsite with no remote work. The co-op runs from January 18, 2027 through June 25, 2027, and applicants must be available for the full duration.
Salary: $20.00–$60.00 per hour, with potential eligibility for discretionary bonus, incentive compensation, or equity subject to plan criteria.
Company
hirify.global develops mRNA technology and biopharmaceutical manufacturing capabilities to support the creation and delivery of medicines.
What you will do
Support digital, automation, controls, software, data, and manufacturing systems in a regulated GMP environment.
Develop, configure, integrate, test, and deploy applications, APIs, data products, dashboards, reports, and automation solutions.
Work with PCS, MES, data platforms, PLC-based systems, databases, and reporting tools.
Troubleshoot data-flow issues, review trends, gather technical evidence, and support investigations.
Document system configurations, data flows, business processes, troubleshooting steps, and standard work.
Support user acceptance testing, regression testing, validation, GMP documentation, and continuous improvement with cross-functional teams.
Requirements
Current enrollment in a bachelor's or master's program in Engineering, Computer Science, Data Science, Information Technology, Biotechnology, or a related technical field.
Basic knowledge of programming, databases, APIs, automation, controls, version control, or information systems.
Experience analyzing data with Python, Power BI, Tableau, Grafana, or a similar tool.
Strong analytical, troubleshooting, communication, independent-working, and cross-functional collaboration skills.
Must already hold U.S. work authorization and maintain it without future sponsorship.
Only U.S. persons eligible under U.S. export-control requirements; visa sponsorship is not available.
Nice to have
GPA of 3.5/4.0 or equivalent.
Experience with data integrity, traceability, validation, ISA-95, change management, or GMP manufacturing.
Exposure to MES, PCS, data historians, SCADA, SQL, ERP, and PLC-based automation systems.
Hands-on coursework, projects, research, internships, open-source contributions, or a technical portfolio involving integration, automation, or software development.
Culture & Benefits
In-person, site-based collaboration with Automation, Manufacturing, Digital, Quality, and Engineering teams.
Hands-on mentorship and exposure to modern biopharmaceutical manufacturing technologies.
Paid time off including vacation, sick time, holidays, volunteer days, and a discretionary year-end shutdown.
Subsidized commuter benefits, location-specific perks, and premium access to meditation and mindfulness classes.
Smoke-free, alcohol-free, and drug-free work environment.
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